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Advocacy Updates

Book with title The Americans with Disabilities Act (ADA).
Blog Post

Recent Updates with Section 504

By Shannon Wood and Joel Cartner | February 11, 2026
Blog Post

Our 2026 Advocacy Agenda

By Mark Fisher | February 5, 2026
2025 MDA Clinical & Scientific Conference - NMAC Meeting - TS
Blog Post

Collective Advocacy at the MDA Clinical & Scientific Conference Propels Hope and Possibility

By Paul Melmeyer | January 8, 2026
Newborn heel prick test and lood puncture, Taking a Heel Blood Sample From Newborn Baby
Blog Post

Families Are Waiting

By Sharon Hesterlee, PhD, President & CEO, Muscular Dystrophy Association | December 23, 2025
Blog Post

Reflecting on 2025’s Advocacy Accomplishments

By Mark Fisher | December 18, 2025
Blog Post

MDA Updates on Air Travel Advocacy

By Shannon Wood | December 3, 2025
Blog Post

A Government Shutdown Couldn’t Stop Advocates During MDA on the Hill 2025

By Mark Fisher | November 25, 2025
A heartwarming scene shows a caregiver pushing a wheelchair through a serene park filled with vibrant nature
Blog Post

5 Things Advocates Should Know: The Alleviating Barriers for Caregivers Act

By Shannon Wood | November 17, 2025
Team of professional doctors and nurses examining newborn baby at the hospital. Healthcare and medicine concept.
Blog Post

MDA Advocacy Team Reports Updates in Newborn Screening Legislation

By Paul Melmeyer | September 4, 2025
Asian kids with disability in special school classroom with Autism child and attractive teacher.
Blog Post

Understanding MDA Advocacy’s Education Policy Efforts

By Jori Houck | July 7, 2025
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Chicago, IL 60607
800-572-1717 | ResourceCenter@mdausa.org

 

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The Muscular Dystrophy Association (MDA) is a qualified 501(c)(3) tax-exempt organization. ©2022, Muscular Dystrophy Association Inc. All rights reserved.

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